Gene: NRAS ×
Source: CLINVAR ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913237
rs121913237
NRAS
12 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 0.700 1.000 9 2006 2016
dbSNP: rs121913250
rs121913250
NRAS
12 0.683 0.440 1 114716127 missense variant C/A;G;T snv 0.700 1.000 9 2006 2016
dbSNP: rs11554290
rs11554290
NRAS
25 0.583 0.600 1 114713908 missense variant T/A;C;G snv 0.700 1.000 8 2006 2016
dbSNP: rs121434595
rs121434595
NRAS
13 0.708 0.320 1 114716124 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs121434596
rs121434596
NRAS
14 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs121913255
rs121913255
NRAS
19 0.667 0.400 1 114713907 missense variant T/A;G snv 0.700 1.000 1 2016 2016